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Ontology Browser

Term:
Friedreich ataxia 2 (DOID:0111219)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Friedreich ataxia +     
Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined 
Friedreich ataxia 1 +   
Friedreich ataxia 2 
A Friedreich ataxia that has_material_basis_in mutation in the 9p23-p11 chromosome region. (DO)
Friedreich Ataxia Congenital Glaucoma 
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness 

Synonyms
Exact Synonyms: FRDA2
Primary IDs: MESH:C566594
Alternate IDs: OMIM:601992
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/11523563 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.